Canonical Allele Identifier: CA350826986

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368393T>A (hg19) ; chr2:g.224503676T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503676T>A , CM000664.2:g.224503676T>A	GRCh38
NC_000002.11:g.225368393T>A , CM000664.1:g.225368393T>A	GRCh37
NC_000002.10:g.225076637T>A	NCBI36
NG_032169.1:g.86722A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1353A>T MANE Select	ENSP00000264414.4:p.Glu451Asp
ENST00000264414.8:c.1353A>T	ENSP00000264414.4:p.Glu451Asp
ENST00000344951.8:c.1155A>T	ENSP00000343601.4:p.Glu385Asp
ENST00000409096.5:c.1281A>T	ENSP00000387200.1:p.Glu427Asp
ENST00000409777.5:c.1281A>T	ENSP00000386525.1:p.Glu427Asp
ENST00000481135.1:n.649A>T
ENST00000617432.4:c.77A>T	ENSP00000477851.1:p.Lys26Ile
NM_001257197.1:c.1155A>T	NP_001244126.1:p.Glu385Asp
NM_001257198.1:c.1371A>T	NP_001244127.1:p.Glu457Asp
NM_003590.4:c.1353A>T	NP_003581.1:p.Glu451Asp
XM_006712800.2:c.1320A>T	XP_006712863.2:p.Glu440Asp
XM_011511994.1:c.1206A>T	XP_011510296.1:p.Glu402Asp
XM_011511995.1:c.1311A>T	XP_011510297.1:p.Glu437Asp
XM_011511996.1:c.1161A>T	XP_011510298.1:p.Glu387Asp
XM_011511997.1:c.1053A>T	XP_011510299.1:p.Glu351Asp
XM_011511994.3:c.1206A>T	XP_011510296.1:p.Glu402Asp
XM_011511996.2:c.1161A>T	XP_011510298.1:p.Glu387Asp
NM_003590.5:c.1353A>T MANE Select	NP_003581.1:p.Glu451Asp
NM_001257198.2:c.1371A>T	NP_001244127.1:p.Glu457Asp
NM_001257197.2:c.1155A>T	NP_001244126.1:p.Glu385Asp